Join ABHI’s Regulatory team for a short 30-minute member webinar to discuss the MHRA’s consultation on the proposal for indefinite recognition of CE-marked medical devices and IVDs in Great Britain. During the session we will outline our current interpretation of the consultation, highlight the key considerations for industry, and invite any final views from members ahead of ABHI submitting its sector response. This is intended as an open forum to ensure outstanding questions, concerns, or practical implications are captured. Members are also encouraged to respond directly to the consultation.

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